Sr Clinical Project Manager

Scientific Search; Ewing Township (NJ); Hybrid; USD 120,000 - 180,000; Full time

Benefits offered by this job

Competitive salary

Comprehensive benefits

Growth-focused environment

Job summary

A leading clinical research organization is seeking a Senior Clinical Project Manager to lead complex global trials in Pennington, NJ. This role involves managing projects from development through closeout, ensuring compliance, and optimizing operational performance. Candidates should possess a Bachelor's degree in life sciences and expertise in GCP, ICH, and clinical trial systems. An environment focused on growth and comprehensive benefits awaits.

Qualifications

• Bachelor's degree in life sciences, pharmacy, nursing, or related field (advanced degree preferred).
• Strong knowledge of GCP, ICH, FDA, and EMA requirements.
• Expertise with CTMS, EDC, and clinical trial systems.
• Financial and vendor management acumen.
• Confident leader in fast-paced, multi-study environments.

Responsibilities

• Lead clinical trials from protocol development through closeout.
• Own project plans, timelines, budgets, and risk mitigation strategies.
• Manage CROs, vendors, sites, and investigator relationships.
• Ensure inspection readiness, regulatory compliance, and data integrity.
• Optimize patient recruitment, retention, and operational performance.
• Provide mentorship and leadership across clinical teams.

Skills

GCP knowledge

Regulatory compliance

Project management

Leadership

Clinical trial systems expertise

Leadership

Education

Bachelor's degree in life sciences, pharmacy, nursing or related field

Tools

CTMS

EDC

Regulatory submission tools

Job description

Overview

Senior Clinical Project Manager Location: Onsite – Pennington, NJ Hybrid

Step into a high-impact role where your work directly shapes the future of innovative therapies for rare and serious diseases. My client is advancing a cutting-edge clinical pipeline, and this role sits at the center of translating bold science into meaningful patient outcomes. You’ll lead complex global trials while influencing how clinical operations scale and evolve.

Why You Should Apply

• Drive end-to-end clinical trials that can redefine standards of care
• Play a visible role partnering with senior leadership and key stakeholders
• Lead CROs, vendors, and cross-functional teams with real decision-making authority
• Contribute to building systems, SOPs, and operational excellence from the ground up
• Competitive salary range and bonus!
• Comprehensive benefits and growth-focused environment

What You’ll Be Doing

• Lead clinical trials from protocol development through closeout
• Own project plans, timelines, budgets, and risk mitigation strategies
• Manage CROs, vendors, sites, and investigator relationships
• Ensure inspection readiness, regulatory compliance, and data integrity
• Optimize patient recruitment, retention, and operational performance
• Provide mentorship and leadership across clinical teams

About You

• Bachelor’s degree in life sciences, pharmacy, nursing, or related field (advanced degree preferred)
• Strong knowledge of GCP, ICH, FDA, and EMA requirements
• Expertise with CTMS, EDC, and clinical trial systems
• Financial and vendor management acumen
• Confident leader in fast-paced, multi-study environments

How To Apply

We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to [e-mail] and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19719.